| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:51023032-51023406 | Rare:214 | ||||
| chr20:51399320-51399860 | Common:6; Rare:224 | ||||
| chr20:51542544-51542892 | Common:18; Rare:263 | ||||
| chr20:51562826-51563051 | Common:1; Rare:35 | ||||
| chr20:51768003-51768727 | Common:15; Rare:421 | ||||
| chr20:51801279-51801860 | Common:14; Rare:225 | ||||
| chr20:51802326-51802765 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:52191120-52191369 | Common:5; Rare:72 | ||||
| chr20:52191406-52191970 | Common:1; Rare:261 | ||||
| chr20:52192087-52192480 | Common:3; Rare:155 | ||||
| chr20:52972121-52972605 | Common:9; Rare:250 | ||||
| chr20:53592989-53593417 | Common:2; Rare:285 | ||||
| chr20:53593456-53593953 | Common:6; Rare:346 | ||||
| chr20:54070328-54070885 | Common:13; Rare:184 | ||||
| chr20:54173801-54174592 | Common:24; Rare:401; Clinvar:4; Clinvar (benign):2 |